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Sponsors

At UCI Health, we recognize that every clinical research project is unique and requires tailored support for our clinical trial partners. We provide a comprehensive range of services that meet the specific needs of each project, whether it's a first-in-human study or a post-marketing clinical trial. If you are a sponsor interested in activating a trial at UCI Health, let us help you through the process. Whether you need assistance with cancer, non-cancer or regenerative medicine clinical trials, our experienced and high-performance teams are here to support you.

Home Clinical Trials Sponsors
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Cancer

At the Chao Family Comprehensive Cancer Center, we provide high-quality and efficient support to develop, activate and complete cancer clinical trials.
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Non-Cancer

At the UCI Center for Clinical Research (CCR), we lead, support and execute innovative clinical trials for a full range of non-cancer conditions to advance medical knowledge.
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Stem Cell & Gene Therapy

At the UCI Alpha Clinic, we provide a centralized unit to enhance stem cell and gene therapy — also known as regenerative medicine — clinical research and activities.
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Why choose UCI Health for your clinical trials?

At UCI Health, we offer an exceptional platform for clinical trials, providing you with unparalleled expertise, state-of-the-art facilities, and a commitment to advancing medical science.

Unmatched expertise and innovation

As an academic medical center with world-renowned experts, we offer unparalleled reliability and a rigorous, efficient approach to clinical trial management. We combine extensive clinical and research expertise with the innovative enterprise at the University of California, Irvine, accelerating the business of clinical trials and expanding access to breakthrough therapies swiftly and safely.

We offer a full range of clinical skills and expertise. As a tertiary care facility, we provide both general care and specialized expertise in rare and difficult-to-treat diseases.

Our dedicated research teams continuously push the boundaries of scientific knowledge, ensuring your clinical trials benefit from the latest advancements and methodologies.

Comprehensive operational support

We provide deep expertise and comprehensive support for initiating and executing clinical trials. We ensure seamless execution and adherence to the highest standards for each phase of your clinical trial.

We also coordinate interactions with patients and partners across all UCI Health hospitals and clinics, our regional partners CHOC Children’s Hospital of Orange County, the Long Beach Veteran Administration Hospital, and the University of California, which gives your clinical trial the support of the entire UC System.

Community engagement and patient care

We engage with local, regional, and national communities, focusing on delivering the highest level of care inclusive to all. Our diverse patient population enhances the generalizability of trial results and accelerates patient recruitment.

According to recent statistics, Orange County’s population is:

  • 40% Hispanic or Latino
  • 29% White
  • 21% Asian
  • 2% Black or African American
  • 2% from other races

State-of-the-art facilities

UCI Health offers state-of-the-art, world-class facilities equipped with the latest technologies to support advanced medical care and clinical research. Our spaces are meticulously designed to ensure the highest standard of patient care, featuring comprehensive services such as imaging, infusion centers, and climate-controlled rooms across multiple hospitals and community clinics in Orange County.

These facilities provide a controlled environment that enhances the accuracy and reliability of your trial outcomes, with precise data collection and analysis at the forefront of our mission.

Proven track record

As a high-performing, top-enrolling site for numerous trials, we have a track record of successful clinical trial management that keeps both the largest pharmaceutical and smallest biotech companies continuing their partnerships with us. Our commitment to excellence and reliability makes us a trusted partner in advancing medical knowledge and improving patient outcomes.

We are dedicated to ensuring your trial begins swiftly and successfully.

Testimonial of Jacob Schlarman
Jacob Schlarman, MBA — Clinical Project Manager, CIT Clinical Trial & Consulting Services

"Each person from the UC Irvine team that we've interacted with has been nothing but positive, flexible and understanding of our common goals."

Read CTI's story
Testimonial of Robert Besthof
Robert Besthof, MIM — Chief Commerical Officer and Head of Operations, NeuroRx

"Aside from the clinical excellence, one of the many aspects that attracted us to your site is your stewardship and sense of urgency."

Read More About NeuroRx

Contact Our Business Development Specialist

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Privacy Policy

University of California, Irvine - Study Information Sheet

UCI Center for Clinical Research Potential Participant Database

Lead Researcher
Maheswari Senthil, MD
UCI Center for Clinical Research

In the instance of parental permission, “You” refers to “Your child.”

  • Please read the information below and ask questions about anything that you do not understand. A
    researcher listed above will be available to answer your questions.
  • You are being asked to participate in a clinical research potential participant database to identify
    potential clinical research studies you may be eligible for. Participation in this database is voluntary.
    You may choose to skip any question. You may refuse to participate or discontinue your involvement
    at any time without penalty or loss of benefits. You are free to withdraw from this database at any
    time. If you decide to withdraw from this database you should notify the research team
    immediately    .
  • You are eligible to participate in this study if you may be interested in participating in a research trial at UCI Health
  • We would like to interview you to learn more about your eligibility for current clinical research studies at UCI. The interview will last about 5-30 minutes, depending on the extent of your medical history.
  • Possible risks/discomforts associated with the database are hearing about potential clinical research studies that may not be of interest to you, invasion of your privacy, or a potential breach of confidentiality.
  • There are no direct benefits from participation in the database. However, this database may help inform you on clinical research studies that you may be eligible for. Participation in UCI clinical research studies help us gain important data and knowledge that may lead to improved treatment options for people with similar conditions to you in the future.
  • There are no alternative procedures available. The only alternative is not to participate in this study.
  • There is no compensation for your participation in this database.
  • There is no cost to you for participation in this database.
  • All information collected will be stored confidentially in a world-class securely-hosted application, “RealTime CTMS,” with robust data protections and encryption. This application has HIPAA compliant architecture and application rules to ensure data privacy and regulatory compliance.
  • Researchers will use your information to assess your eligibility for current and future clinical research studies at UCI. You may opt out at any time.
  • The research team, authorized UCI personnel, and regulatory entities, may have access to your study records to protect your safety and welfare.
  • While the research team will make every effort to keep your personal information confidential, it is possible that an unauthorized person might see it. We cannot guarantee total privacy.
  • Future Research Use
    Researchers will use your information to conduct this study. Once the study is done using your information, we may share them with other researchers so they can use them for other studies in the future. We will not share your name or any other private identifiable information that would let the researchers know who you are. We will not ask you for additional permission to share this de-identified information
  • Data Retention - In accordance with UC Office of the President policy, information will be retained for 10 years after the end of the calendar year in which the research is completed.
  • If, during the course of this study, significant new information becomes available that may relate to your willingness to continue to participate, this information will be provided to you by the research team listed at the top of the form.
  • If you have any comments, concerns, or questions regarding the conduct of this research please contact the researchers listed at the top of this form
  • Please contact the UCI Institutional Review Board by phone, (949) 824-8170, by e-mail at IRB@research.uci.edu or at 160 Aldrich Hall, Irvine, CA 92697-7600 if you are unable to reach the researchers listed at the top of the form and have general questions; have concerns or complaints about the research; have questions about your rights as a research subject; or have general comments or suggestions.
What is an IRB? An Institutional Review Board (IRB) is a committee made up of scientists and nonscientists. The IRB’s role is to protect the rights and welfare of human subjects involved in research. The IRB also assures that the research complies with applicable regulations, laws, and institutional policies. UCI